FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10603295126010 · Model: 2492-58-000 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10603295126010
Version / Model
2492-58-000
Catalog Number
249258000
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-30
Public Version
4
Public Version Date
2019-08-02
Public Version Status
Update
Public Device Record Key
2987c00e-8c07-457a-95b8-c02dab13ba62

Device Description

KNEE UNIVERSAL INSTRUMENT TIBIAL RESECTION BLOCK 10 DEGREES

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HTZ INSTRUMENT, CUTTING, ORTHOPEDIC

GMDN Terms

Code Name
44742 Joint prosthesis implantation kit, reusable

Identifiers

Type ID
Primary 10603295126010

Customer Contacts